Product NDC: | 62742-4039 |
Proprietary Name: | SUN Solar Defense Oil-free Gel SPF 15 |
Non Proprietary Name: | Titanium Dioxide, Ethylhexyl Methoxycinnamate, Benzophenone-3 |
Active Ingredient(s): | 75; 30; 16 mg/mL; mg/mL; mg/mL & nbsp; Titanium Dioxide, Ethylhexyl Methoxycinnamate, Benzophenone-3 |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62742-4039 |
Labeler Name: | Allure Labs, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100101 |
Package NDC: | 62742-4039-1 |
Package Description: | 118 mL in 1 TUBE (62742-4039-1) |
NDC Code | 62742-4039-1 |
Proprietary Name | SUN Solar Defense Oil-free Gel SPF 15 |
Package Description | 118 mL in 1 TUBE (62742-4039-1) |
Product NDC | 62742-4039 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide, Ethylhexyl Methoxycinnamate, Benzophenone-3 |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Allure Labs, Inc. |
Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | 75; 30; 16 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |